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Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 2005 Feb;43(2):898–902. doi: 10.1128/JCM.43.2.898-902.2005

Persistence of Escherichia coli O157 Isolates on Bovine Farms in England and Wales

Ernesto Liebana 1,*, Richard P Smith 2, Miranda Batchelor 1, Ian McLaren 1, Claire Cassar 1, Felicity A Clifton-Hadley 1, Giles A Paiba 2
PMCID: PMC548034  PMID: 15695700

Abstract

We performed pulsed-field gel electrophoresis on Escherichia coli O157 isolates (n = 318) from 199 healthy animals in a longitudinal study carried out on nine farms. Investigation of the restriction types proved that at the farm level, the same clones can be detected on sampling occasions separated by as much as 17 months. The cohort animals were repeatedly sampled, and for some of these, the same clones were obtained on sampling occasions separated by as much as 8 months.


Escherichia coli strains that produce Shiga-like toxins, also known as verocytotoxins, have been implicated as the cause for human disease (hemorrhagic colitis and hemolytic-uremic syndrome). One particular serovar, E. coli O157, represents a major public health concern worldwide. Healthy asymptomatic cattle are the best-recognized animal reservoir for these organisms, and shedding via feces occurs only intermittently, typically lasting 3 to 4 weeks (5, 10, 16). Several molecular techniques have been used to investigate the epidemiology of E. coli O157, and pulsed-field gel electrophoresis (PFGE) is currently considered the “gold standard” for DNA fingerprinting of these strains (17). The ecology and epidemiology of this organism in cattle appear to be very complex, often involving multiple clones on a single farm (9, 14). There is some previously published information about on-farm persistence in different cattle production systems (8, 15, 16). However, the information about persistence in individual animals is very scarce. A longitudinal study was conducted to provide information on the persistence and maintenance of colonization with E. coli O157 at the farm level as well as the individual-animal level in the context of a typical farm in the United Kingdom.

Bacterial strains.

E. coli O157 isolates (n = 648) were cultured from bovine fecal samples from nine epidemiologically unrelated farms dispersed across England and Wales (9, 12). All the isolates were confirmed as serotype O157 by serum agglutination (11); the first confirmed colony from a positive sample was selected as representative for that animal and was stored at −80°C. The first sampling visit occurred during the months of August to November 1999 and used previously described epidemiological methods (12). The longitudinal study started in April 2000; during the first visit, as many as 90 animals under the age of 24 months (“original cohort”) were randomly selected for sampling on each farm selected. Subsequently, monthly sampling visits were carried out until February 2001. Samples of rectal feces (one per animal) were collected from individuals in the original cohort, as well as from any cattle born since the previous visit and any new acquisitions to the herd.

A total of 318 E. coli O157 isolates from 199 healthy bovines on nine farms were characterized by PFGE (Table 1). This selection covered all isolates from animals that yielded two or more positive results on several sampling occasions, as well as a random representation of isolates from animals that were found to be positive only on one occasion. These comprised 29 to 100% of the available isolates for each of the farms. Preparation and XbaI digestion of DNA for PFGE and analysis of results were conducted as described previously (2).

TABLE 1.

E. coli O157 isolations by farm and sampling date

Site No. of animals sampled (no. positive for E. coli O157) at the following timea:
No. (%)b of isolates typed by PFGE
08/99 to 11/99 04/00 05/00 06/00 07/00 08/00 09/00 10/00 11/00 12/00 01/01 02/01
Farm 2 80 (38) NS 90 (8) 92 (4) 90 (4) 90 (5) NS 90 (1) 91 (12) 90 (53) 90 (30) 86 (28) 111 (60)
Farm 3 46 (12) NS 56 (23) 53 (14) 61 (1) 46 (0) 54 (7) 57 (0) 61 (0) 60 (0) 60 (0) 60 (0) 35 (61)
Farm 4 57 (9) NS 72 (5) 26 (1) 23 (4) 23 (7) 42 (8) 74 (13) 92 (11) NS 92 (15) 92 (7) 27 (34)
Farm 5 64 (1) NS 89 (7) 75 (8) 83 (2) 98 (4) 135 (4) 87 (1) NS NS NS NS 8 (29)
Farm 6 87 (11) 90 (2) 48 (0) 55 (0) NS 58 (0) 63 (1) 88 (0) 90 (1) 91 (1) 88 (0) 87 (2) 10 (55)
Farm 8 46 (5) 90 (11) 83 (43) 82 (17) 80 (6) 53 (14) 54 (8) 58 (1) 62 (3) 90 (3) 112 (12) NS 37 (30)
Farm 9 72 (37) 90 (0) 93 (0) 90 (1) 91 (35) 92 (23) 92 (23) 101 (9) 102 (9) 101 (8) 101 (0) 90 (0) 78 (54)
Farm 10 46 (5) 31 (0) 40 (0) 41 (0) 45 (0) 40 (0) 36 (0) 33 (0) 32 (0) NS 33 (1) 33 (1) 4 (57)
Farm 11 61 (4) NS NS 37 (0) NS 35 (0) 37 (0) 38 (0) 41 (0) 40 (2) 41 (1) 41 (1) 8 (100)
a

Sampling dates are given as month/year. NS, no sampling was conducted.

b

Percentage of the total isolates available for a given farm that was typed.

Table 2 details the persistence of PFGE subtypes at the farm level. The most persistent types (X49 and X25) were isolated from samples from farms 4 and 8, taken 17 and 16 months apart, respectively. Types X8 and X24 were found in isolates from farms 8 and 9, respectively, on six consecutive sampling occasions. On every farm, a variety of types were found on particular sampling occasions and never found again. This situation does not seem to be unique to the United Kingdom; previous work from the United States indicates that individual strains can be isolated from some dairy herds for as long as 2 years (16), for as long as 10 months in cattle ranges (15), and over the entire feeding period on cattle feedlots (8).

TABLE 2.

On-farm persistence of PFGE types

Site PFGE type isolated at the following time (mo/yr)a:
08/99 to 11/99 04/00 05/00 06/00 07/00 08/00 09/00 10/00 11/00 12/00 01/01 02/01
Farm 2 NS NS X39 X39 X39 X39
NS NS X44 X44 X44 X44 X44
NS NS X45 X45 X45
Farm 3 X24 NS X24 X24 X24 X24
NS X26 X26
Farm 4 X49 NS X46 NS X46 X46
X49 NS X49 X49 X49 X49 NS X49
NS X50 X50 NS
NS X52 X52 NS
NS X54 X54 NS X54
Farm 5 NS X31 X31 NS NS NS NS
NS X56 X56 NS NS NS NS
Farm 6 X22 X22 NS
NS X42 X42
Farm 8 X8 X8 X8 X8 X8 X8 NS
X25 X25 X25 X25 NS
X30 X30 X30 X30 X30 X30 NS
Farm 9 X24 X24 X24 X24 X24 X24
X26 X26 X26
X27 X27 X27 X27
Farm 10 NS X24 X24
Farm 11 NS NS NS X8 X8
a

−, E. coli O157 was not isolated from the premises. NS, the farm was not sampled on that occasion. An empty cell indicates that E. coli O157 isolates were obtained, but they presented PFGE types that were never found again on that farm at any sampling time.

Table 3 shows a summary of the types persisting in animals that were positive for E. coli O157 on two or more sampling occasions. In most cases, several different PFGE types were found persisting in different animals from the same farm. However, in one case (farm 3), the same clone persisted in all the animals for which persistence could be demonstrated. The most persistent clone at the individual-animal level was X24, which was found in isolates recovered from samples from animals 13 and 17 on farm 3, taken 7 months apart. On several occasions (animal 156, farm 2; animal 56, farm 8; animal 9, farm 9) the same clones were found on four consecutive sampling occasions. Types X44 and X45, X46 and X47, and X8 and X11 were very similar; each of these pairs differed only in ≤2 restriction fragments (Fig. 1). For this reason, they have been included in Table 3. One suspects that these variations may be due to clonal turnover in the animal. Similar small variations in PFGE profiles have been reported before in experimental and natural infections (1, 6).

TABLE 3.

Persistence of PFGE types in individual animals that were positive for E. coli 0157 on two or more occasions and from which a PFGE result was available

Farm Animal PFGE type isolated at the following time (mo/yr)a:
08/99 to 11/99 04/00 05/00 06/00 07/00 08/00 09/00 10/00 11/00 12/00 01/01 02/01
Farm 2 A133 NS NS NS NS NS NS X44 X44 NS NS
A151 NS NS NS NS NS NS NS
A156 NS NS NS NS NS NS X39 X39 X39 X39
A162 NS NS NS NS NS NS X39 X39
A166 NS NS NS NS NS NS X39 X39 NS
A179 NS NS NS NS NS NS NS X44 X44
A196 NS NS NS NS NS NS NS X44 X45
A206 NS NS NS NS NS NS NS NS
A207 NS NS NS NS NS NS NS NS X44 X44
A208 NS NS NS NS NS NS NS NS
A210 NS NS NS NS NS NS NS NS X44 X45
A212 NS NS NS NS NS NS NS NS X44 X44
A215 NS NS NS NS NS NS NS NS X44 X44
A217 NS NS NS NS NS NS NS NS X44 X45
A219 NS NS NS NS NS NS NS NS X44 X44
A225 NS NS NS NS NS NS NS NS
A230 NS NS NS NS NS NS NS NS X39 X39
A247 NS NS NS NS NS NS NS NS NS NS X39 X39
A259 NS NS NS NS NS NS NS NS NS NS X44 X45
A260 NS NS NS NS NS NS NS NS NS NS X44 X45
A265 NS NS NS NS NS NS NS NS NS NS X44 X44
A268 NS NS NS NS NS NS NS NS NS NS X44 X44
Farm 3 A4 NS NS NS NS NS NS NS NS
A10 NS NS NS NS NS NS NS NS
A13 X24 NS X24 NS NS NS NS NS NS NS NS
A17 X24 NS X24 X24 NS NS NS NS NS NS
A19 NS NS NS NS NS NS NS NS NS NS
A21 NS NS X24 X24 NS NS NS NS NS NS NS NS
A26 NS NS NS NS NS NS NS NS NS NS
A28 NS NS X24 X24 NS NS NS NS NS
A32 NS NS NS NS NS NS NS NS NS NS
A35 NS NS NS NS NS NS NS NS NS NS
A36 NS NS X24 X24 NS NS NS NS NS NS NS NS
A40 NS NS NS NS NS NS
A45 NS NS NS NS NS NS NS
A53 NS NS NS NS NS NS NS
A55 NS NS NS NS NS NS
Farm 4 A2 NS NS X52 X52 NS
A5 NS NS X49 X49 NS
A6 NS NS X54 X54 NS
A8 NS NS NS
A18 NS NS NS X49 X49 NS
A21 NS NS X49 NS X49
A79 NS NS NS NS NS NS NS NS X46 NS X46
A82 NS NS NS NS NS NS NS NS NS
A92 NS NS NS NS NS NS NS NS NS X46 X47
Farm 5 A19 NS NS X56 NS X56 NS NS NS NS
A41 NS NS X31 X31 NS NS NS NS NS NS NS
A43 NS NS NS NS NS NS NS NS NS NS
Farm 8 A17 NS X8 X8 X8 NS NS NS NS NS NS NS
A22 NS X8 X11 X8 NS NS NS NS NS NS NS
A23 NS X8 X8 NS NS NS NS NS NS NS
A24 NS X8 X8 X8 NS NS NS NS NS NS NS
A48 NS X30 X30 NS NS NS NS NS NS NS NS
A56 NS X30 X30 X30 X30 NS NS NS NS NS NS NS
A78 NS X30 X30 NS NS NS NS NS NS NS
A93 NS NS X8 X8 NS NS NS NS NS NS
A102 NS NS NS X8 X8 NS NS NS NS
A104 NS NS NS NS NS NS NS NS
A138 NS NS NS NS NS X30 X30 NS NS NS NS
A193 NS NS NS NS NS NS NS NS X25 X25 NS
Farm 9 A3 NS NS
A7 NS
A9 NS X24 X24 X24 X24 NS
A16 NS NS NS NS NS
A29 NS X24 X24 X24 NS NS NS
A31 NS X24 X24 X24 NS
A47
A53
A56 NS X27 X27 X27
A59 X24 X24
A74 NS X24 X24
A77 NS
A81 NS X26 X26
A82 NS X25 X26
A92 NS NS
A93 NS NS X24 X24
Farm 10 A39 NS NS NS NS NS X24 X24
Farm 11 A5 NS NS NS NS X8 X8
A13 NS NS NS
a

−, the sample from the animal was negative for E. coli O157. NS, the animal was not sampled on that occasion. Empty cells indicate that the sample from the animal was positive for E. coli O157, but the isolates showed fingerprints that were never found again in isolates from the same animal.

FIG. 1.

FIG. 1.

Dendrogram generated with Bionumerics software showing the PFGE XbaI types for three pairs of E. coli O157 isolates. The bands generated were analyzed by using the Jaccard coefficient and the unweighted-pair group method with arithmetic averages. Molecular weights (in kilobase pairs) are given above the gel.

A study from Australia showed that indistinguishable PFGE types could be consistently isolated from cattle feces for as long as 49 days (10). However, it also seems true that individual animals may shed multiple strains simultaneously, and the spectrum of types changes over time (7). Some studies have indicated that E. coli O157 strains seem to be continually replaced by new and distinct types in cattle (4, 13). This agrees with the results in our study, where on several occasions, animals appeared to shed different types at different times. All of this seems to indicate that E. coli O157 strains cycle with a high turnover through individual cattle, though predominant strains may persist collectively on a farm (3).

We are aware that the selection of only a fraction of our isolates for PFGE, as well as the fact that only one colony per positive animal was stored, may have influenced our results. However, in spite of these limitations, we have successfully demonstrated that some clones can be isolated from the same farms over a period of at least 17 months and from the same animal over a period of at least 7 months. We cannot be sure if these results are a reflection of persistent colonization of the animal by a particular clone or if they are due instead to residual contamination of the farm environment and recycling through the host. In any case, we have demonstrated that defined PFGE clones persist on farms in the United Kingdom for a significant period. In most cases, the persisting types coincided with the most prevalent clones for the farm (9), indicating that less prevalent clones may represent only transient episodes of contamination.

Acknowledgments

We thank Tom Cheasty and Geraldine Willshaw (PHLS, Colindale, United Kingdom) for phage typing of the strains.

This work was supported by DEFRA grant OZ0138.

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